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NCT ID: NCT04278196 Completed - Clinical trials for Magnet Controlled Capsule Endoscopy

Computer Assisted Quality-monitoring for Magnet-controlled Capsule Endoscopy: a Prospective Case-control Study.

Start date: January 1, 2020
Phase:
Study type: Observational [Patient Registry]

During the past several years,MCE(magnet controlled endoscopy)has made great process in detecting lesions of gastric as well as screening. Compared with conventional endoscopy, magnetically controlled capsule endoscopy can be further optimized in gastric examination. So we make an AI for operators to help improve the quality of MCE and record the mucosa visibilty of gastirc.

NCT ID: NCT04278079 Completed - Clinical trials for Pars Plana Vitrectomy

Vitrectomy With Internal Limiting Membrane Peeling for Myopic Traction Maculopathy

Start date: January 2015
Phase: N/A
Study type: Interventional

Investigate the effectiveness and safety of pars plans vitrectomy, with internal limiting membrane peeling for cases of myopic traction maculopathy

NCT ID: NCT04278053 Completed - Clinical trials for Determine the Effects of Nitrosigine and Citrulline-malate on Flow-mediated Dilation Among Young Adults

Evaluation of Sports Supplements on Blood Flow

Start date: October 15, 2018
Phase: N/A
Study type: Interventional

Many athletes seek to increase their plasma (blood) nitric oxide content prior to exercise in order to augment vasodilation. Increased vasodilation during exercise, especially high intensity resistance training, allows for more blood flow to muscle tissues, which may give the athlete benefits such as increased work capacity and acute muscle hyperemia, which is commonly referred to as muscle pump. Pre-workout supplements are typically taken 30 minutes to 1 hour prior to the onset of exercise, so the current investigation seeks to determine if citrulline malate or nitrosigine can effect vasodilation within 1 hour of supplementation, and if so, which supplement is more effective. Based on previous findings, we hypothesize that a certain exercise intensity needs to be present for citrulline malate and nitrosigine to have an effect, so a change may not be observable at rest.

NCT ID: NCT04277286 Completed - Clinical trials for Pediatric Patient Transfer to Adult Service:Transition Program

Evaluation of the TRANSEND Program

EVATRANSEND
Start date: September 9, 2020
Phase:
Study type: Observational

"Transend" is a program designed to promote the transition of young patients with endocrine or metabolic diseases when they arrive in the adult sector at La Pitié-Salpétrière hospital. The main objective of the study is to compare the rate of patients lost to follow-up at 24 months after the transfer of pediatrics between the Transend group and the (historical) control group.

NCT ID: NCT04277169 Completed - Clinical trials for Ultrasound Imaging of Anatomical Structures

A Volunteer Study to Collect Imaging Data for the Development of the IntelligentUltrasound Anatomy Guide

Start date: February 1, 2020
Phase:
Study type: Observational

This is a single-centre, prospective, non-randomised volunteer study to be undertaken in the MediCentre, Heath Park, Cardiff, UK

NCT ID: NCT04276935 Completed - Clinical trials for Human Immunodeficiency Virus

Development of a Health-Related Symptom Index for Participants With and Either Treated or Monitored for Anal High-Grade Squamous Intraepithelial Lesions

Start date: November 6, 2018
Phase:
Study type: Observational

This trial develops a health-related symptom index for participants with and either treated or monitored for anal high-grade squamous intraepithelial lesions. The health-related quality of life index may help to capture the symptoms and related experiences of living with or being treated for high-grade squamous intraepithelial lesions.

NCT ID: NCT04276883 Completed - Bipolar Disorder Clinical Trials

Dexmedetomidine in the Treatment of Agitation Associated With Bipolar Disorder

SERENITY II
Start date: February 24, 2020
Phase: Phase 3
Study type: Interventional

This is a definitive study to support the safety and efficacy evaluation of BXCL501 for the acute treatment of agitation in bipolar disorder. The BXCL501-302 study is designed to characterize the efficacy, safety and tolerability of BXCL501 (sublingual film formulation of DEX, HCl) in agitation associated with bipolar disorder.

NCT ID: NCT04276584 Completed - Clinical trials for Postoperative Respiratory Complications

Effect of Speaking Aloud After Abdominal Surgery.

Start date: February 20, 2020
Phase: N/A
Study type: Interventional

Hypoxia and reduced vital capacity is commonly occurring after abdominal surgery. Positive expiratory pressure is one treatment suggested to improve lung function after surgery. We aim to test whether speaking improves postoperative oxygen saturation and ventilation after abdominal surgery. In a cross-over design, 50 subjects will be randomized to start with either positive expiratory pressure maneuvers, i.e. deep inspiration followed by expiration in a positive expiratory pressure device at 10-15 cm of water, or to start with reading a text loudly. Arterial blood gases will be taken at study start. Patients will be monitored using Noxturnal T3, Res Med for respiration and pulse oximetry, and online transcutaneous carbon dioxide partial pressure measurements (SenTec Digital monitoring systems). Main outcome measurements include oxygen saturation after speaking compared with positive expiratory pressure therapy.

NCT ID: NCT04276194 Completed - Clinical trials for Malignant Central Nervous System Neoplasm

Vertebral Body Sparing Craniospinal Irradiation for Pediatric Patients With Cancer of the Central Nervous System

Start date: December 16, 2019
Phase: N/A
Study type: Interventional

This trial studies the feasibility of using intensity modulated proton therapy to deliver craniospinal irradiation while avoiding the bones of the vertebral column. Intensity modulated proton therapy is an advanced radiation therapy modality that uses high energy protons to kill cancer cells and shrink tumors, and may reduce the side effects of treatment by reducing radiation exposure to the spinal column.

NCT ID: NCT04275960 Completed - Clinical trials for Solid Tumors Harboring NTRK Fusion

Study in Healthy Adult Male Participants to Gather Information How the Human Body Absorbs, Distributes and Excretes the Study Drug Selitrectinib Including the Effect of the Interaction of Food With the Study Drug on the Human Body

Start date: February 28, 2020
Phase: Phase 1
Study type: Interventional

The researchers in this study want to gather information in healthy adult male participants about how the human body absorbs, distributes and excretes the drug selitrectinib including the effect of the interaction of food with the study drug on the human body. Selitrectinib is a new drug under development for the treatment of patients with solid tumor caused by a genetic abnormality known as an NTRK gene fusion which cannot be cured by currently available treatment options or has spread to other parts of the body. The drug blocks the action of the NTRK gene fusion and prevents the activation of certain proteins (TRK fusion proteins), which can cause cancer cells to multiply and form a tumor. Researchers also want to find out if the participants have any medical problems during this study. Participants in this study will receive the study drug twice with at least 6 days in between. The study drug will be taken orally as a liquid before or after meal. Observation will last for up to 8 weeks, and blood samples will be taken from the participants to measure the blood levels of the study drug.